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1-(3-chlorophenyl)-2-phenylhydrazine is an organic compound with the chemical formula C12H10ClN3. It is a derivative of hydrazine, featuring a 3-chlorophenyl group attached to the first carbon atom and a phenyl group attached to the second carbon atom. 1-(3-chlorophenyl)-2-phenylhydrazine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain anti-inflammatory and antimicrobial agents. Due to its reactivity, it is important to handle this chemical with care, as it may pose health risks and requires proper safety measures during its use and storage.

949-73-5

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949-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 949-73-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 949-73:
(5*9)+(4*4)+(3*9)+(2*7)+(1*3)=105
105 % 10 = 5
So 949-73-5 is a valid CAS Registry Number.

949-73-5Relevant academic research and scientific papers

Hydrogen peroxide based oxidation of hydrazines using HBr catalyst

Du, Wanting,Ma, Zichao,Shao, Liming,Wang, Jian

, (2021/11/18)

Azo compounds (RN = NR′) are an important class of organic molecules that find wide application in organic synthesis. Herein, we report an efficient, practical and metal-free oxidation of hydrazines (RNH-NHR’) to azo compounds using 5 mol% HBr and hydrogen peroxide as terminal oxidant. This new method has been demonstrated by 40 examples with excellent yields. In addition, we showcased two examples of the one-pot sequential reactions involving our hydrazine oxidation/hydrolysis/Heck reaction or Cu-catalyzed N-arylation with aryl boronic acid. The distinct advantages of this protocol include metal-free catalysis, waste prevention, and easy operation.

Visible-Light-Promoted Diboron-Mediated Transfer Hydrogenation of Azobenzenes to Hydrazobenzenes

Song, Menghui,Zhou, Hongyan,Wang, Ganggang,Ma, Ben,Jiang, Yajing,Yang, Jingya,Huo, Congde,Wang, Xi-Cun

, p. 4804 - 4811 (2021/04/06)

A visible-light-promoted transfer hydrogenation of azobenzenes has been developed. In the presence of B2pin2 and upon visible-light irradiation, the reactions proceeded smoothly in methanol at ambient temperature. The azobenzenes with diverse functional groups have been reduced to the corresponding hydrazobenzenes with a yield of up to 96%. Preliminary mechanistic studies indicated that the hydrogen atom comes from the solvent and the transformation is achieved through a radical pathway.

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